Dichlorotriazino substituted phthalocyanine dyestuffs



United States Patent 3,507,864 DICHLOROTRIAZINO SUBSTITUTED PHTHALO- CYANINE DYESTUFFS Asa W. Joyce, Millersville, Md., and Julian J. Leavitt,

Plainfield, N.J., assignors to American Cyanamid Company, Stamford, Conn., a corporation of Maine No Drawing. Continuation of application Ser. No.

125,942, July 24, 1961, which is a division of application Ser. No. 781,871, Dec. 22, 1958, now Patent No. 3,055,895, dated Sept. 25, 1962. This application Mar. 25, 1964, Ser. No. 354,757

Int. Cl. C07d 55/12 U.S. Cl. 260248 1 Claim ABSTRACT OF THE DISCLOSURE This invention relates to new dyes of the formula COX &

wherein, in the benzoylene moiety, the remaining carbons are bonded to substituents selected from hydrogen, lower alkyl, lower alkoxy, chlorine, and bromine; Y is selected from chlorine, bromine, and NHR; Z is selected from chlorine, bromine, and NHR'; X is selected from chlorine, bromine, dialkylamino, diethanolamino, N-piperdyl, N-morpholinyl, and NHR; wherein R, R, and R" are each the remainder of an organic dye containing amino groups, such as an amino-azo dye, an amino-vat dye, or an aminophthalocyanine dye, the --NH- moiety at tached thereto being the residue of an amino group of such dye; with at least one of X, Y, and Z containing the remainder of such an organic dye.

A most important feature of the present invention is the linkage of the dye-residues of amino dyes to a novel carboxyphenyltriazine nucleus to produce a novel class of dyes. These novel dyes may be further characterized as ones wherein a benzoylene moiety is linked to a triazine nucleus with at least one dye residue linked to the carbonyl group of the benzoylene moiety or to a triazine carbon.

CROSS REFERENCE TO RELATED APPLICATIONS This application is a continuation of our copending application Ser. No. 125,942 filed July 24, 1961 now abandoned which, in turn, is a division of our application Ser. No. 781,871, filed Dec. 22, 1958, now U.S. Patent No. 3,055,895, issued Sept. 25, 1962.

Dyes containing triazine nucleus have been known in the past several fields of dyestuif chemistry. They have in the past, had in common the characteristic of a direct linkage through an amino group between the dyestuit residue and the triazine ring. They have usually been ilk-C OX N Z LY in which Ar is a residue of the benzene series carrying as additional substituents alkyl, alkoxy or halogen groups, and in which X, Y and Z are hydroxy or halogen, such as chlorine and bromine, are intermediates for the formation of new dyestufis which are exceptional in the ease with which they form such dyestuffs and in the variety of dyestuffs and shades which they may be obtained therefrom. We have further found that the dyestuffs of the similar formula in which at least one of X, Y and Z is the residue of dyestutf linked to the molecule through a replacement of a hydrogen on an amino group are valuable dyestuifs of the vat, azo, direct dye and similar fields. Such dyes could have X, Y and Z represent entirely different dyestuff residues and thus produce composite colors or they can all be the same. Also the intermediate compounds, in which only one or two of X, Y and Z are replaced with a dyestuif residue, are similarly valuable dyestuffs in their own right.

It is an advantage of our invention that these intermediates react more readily with the amino dyestufiis to link a triazine moiety and a dyestutf nucleus into a common molecule. This is of course most especially true of the replacement of X in the above formula since a carbonyl halide reacts more readily than does a triazine halogen. This difference in reactivity further permits the preparation, in a much more clean-cut fashion and with greater ease, of the types of dyestuffs in which there are several diiferent dyestuffs linked to the same triazine molecule and this is a still further advantage of our invention.

It is a further advantage of our invention that the dyestutfs in which X is a color moiety and Y and Z are halogen are stable enough to permit the use of such dyes in high temperature dyeing procedures, a use not normally possible with dichlorotriazinyl dyes. Another advantage of our invention is that other dyes can be prepared (e.g. those in which X is halogen and either or both of Y and Z are dyestufi residues) which have more reactive halogens than normally can be obtained with chlorotriazinylamino dyestuffs. Our invention thus presents an extraordinary flexibility in the dyestufl properties obtainable.

(I) INTERMEDIATES The new intermediates of our invention are prepared from toluguanamides by oxidation with a permanganate to the corresponding carboxybenzoguanamides. These are then subsequently chlorinated to the acid chloride of the carboxyphenyldichlorotriazine. The known starting materials are easily obtained by beginning with an ortho-, meta-, or a para-, toluic acid chloride and reacting it with dicyandiamide. The resulting toluyldicyandiamide is then hydrolyzed to the biuret with acid, and ring-closed to the toluguana-mide by sodium hydroxide in known manner. The preparation of these intermediates is illustrated in more detail by the following series of reactions.

The starting toluic acid chloride may have other substituents present, such as alkyl, alkoxy or halogen. Examples of the toluic acids which may be used are ortho-, meta-, and para-toluic acid, 2-methoxy-5-methylbenzoic acid, 2 chloro methylbenzoic acid, 2 methoxy 4- methylbenzoic acid, 2 chloro 4 methylbenzoic acid, and the like.

In the above equation there is shown the conversion of the benzoguanamide to the corresponding dichlorotriazine derivative. However it is clearly equivalent to use the corresponding phosphorous pentabromide or thionyl bromide in order to form the corresponding bromo compounds and these bromo compounds are included within the scope of our invention.

The groups X, Y and Z in the intermediates of our invention need not all be the same although the species in which they are all alike are the more readily obtainable. However, for example, species in which only X has become chloro or bromo while Y and Z remain hydroxyl can be obtained readily by careful treatment with thionyl chloride under conditions (lower temperature and restricted mole usage of SOCl which do not go on to replace the triazine hydroxyls. Similarly the compound in which X, Y and Z are all chloro or bromo can be hydrolyzed step wise to make X alone or X and Y hydroxyl, leaving the others chloro or bromo. This interconversion is illustrated in the following schematic equations:

@0011 soon 0001 soon -oo0H H20 N N N N N N CILN CI CHLN CI CI-LN OH The various intermediate steps shown can, of course, also be used as dye intermediates by the reaction wlth a dye amine followed by further reaction to form the halogen derivatives. Thus these intermediates of our invention are quite versatile in the preparation of various dyestuffs of the carboxyphenyltriazine type shown in later paragraphs in this specification. Although the above equation shows the m-carboxyphenyl derivative, the reactions occur also with the para and ortho-isomers, as well as with compounds having other substituents on the molecule.

(II) DYESTUFF S The dyestufis which can be prepared from the com pounds of our invention and which form another aspect of our invention are based on the linking of the carboxyphenyltriazine nucleus to residues of dyestuff amines. The linking is achieved through the amino group in a known dyestuif moiety. This linking can be carried out in a stepwise manner. Thus any of the chlorinated carboxyaryltriazines shown in the above equation can be reacted with an amino dyestuff in which the amino group has a replaceable hydrogen and the said hydrogen is replaced by the carboxyphenyltriazine nucleus to form the bond to the dye residue. The carbonyl chloride radical will react first and thus, in those compounds of our invention in Which the carboxyl group has been transformed into the carbonyl chloride, a clean reaction can be obtained to form the dyes in which X is an amino dye residue and Y and Z in the above formulas remain either chlorine, bromine or hydroxy. Under somewhat differing conditions additional halogens on the triazine can be further replaced, still stepwise to get a complete replacement as well as partial replacement of the halogens. This will be discussed in detail later in the specification, after a discussion of the various amino dyestufis which can be used.

At least one of the groups X, Y and Z in the generic formula must be, in the dyestuffs of our invention, a residue of an amino dyestulf linked to the phenyltriazine moiety through the amino group. The amino group on the dye residue may be either a primary or secondary amino grou in the original dye molecule. It cannot be a tertiary amino group since there would be no replaceable hydrogen by whose elimination there could be formed a further covalent bond with the phenyltriazine moiety. The dye residues which may thus be linked to the phenyltriazine nucleus in the dyestuffs of our invention will be described below in much detail. In that discussion, extensive reference will be made to The Chemistry of Synthetic Dyes by K. Venkataraman, Academic Press, New York (1952) and to the American Chemical Society, Monograph No. 127, on the Chemistry of Synthetic Dyes and Pigments by H. H. Lubs, Reinhold, New York 1955). While many of the dyestuff residues which may be used in the dyes of our invention will be described in detail in the specification, in order to provide a complete disclosure these treatises are included expressly by reference in this specification as indicated in the various discussions.

The principal limitations on the dyestutf residues which may be used in forming the dyes of our invention is that these dyestuif residues must contain an amino group capable of forming a further covalent linkage, i.e., an amino group having a replaceable hydrogen. Such a definition includes primary and secondary amino groups and excludes tertiary amino groups. In general, a secondary amine is preferably an alkyl aryl amino compound, since the diaryl amines do not react as well. As described below, all the various classes of dyestuffs can be used, but

through the amino group to the carbonyl group of mcarboxyphenyldichlorotriazine.

those members which are useable have this factor in ISOQNQ H common: no matter what the general class of dyestufi' involved, the dyestuff residue must have a primary or N= secondary amino group which can react with the halogens in the carboxyphenyltriazine nucleus to form the dyestuffs Naots *SOaNa of our invention. In general dyestuffs of similar structure I N N are preferred. L I Cl When water-soluble dyestuffs are desired, the dyestuft N residue should contain an acidic group in order to achieve Such a dyestuff is prepared by reacting one mole of the the proper water olubility Of the acidic groups, the sulaminoazo dye With the dichlorotriazinylbenzoyl chloride. fonate group is of course by far the preferred one with If three moles of the amiheale y are used, all three the carboxylate and sulfonarnide groups the ones most chlormes are lh likely to be used next The azo dye itself may be used for the reaction with the carboxyphenyltriazine derivative. However, in the (A h d t ff residues Azo dyes case of azo dyes especially, there are alternative methods whereby the chlorocarbonylphenyldichlorotriazine may be Azo dyes are described in Venkataraman in chapters first reacted with an amino aromatic compound, to be 11-22, inclusive, pages 409-704, and in Lubs, chapter 3, used as a coupling Component of as a (haze Component pages 95 131 A great many azo d t ff are known to in forming the azo molecule. In the reaction, for example, tha art hi have Primary or Secondary amino groups i of one mole of an aminonaphthol with dichlorotriazinyltheir structure. Such compounds, as described in the benzqyl chloride followed by f s of a (halo compo above-mentioned pages of Venkataraman and Lubs, are heht the haphthol thfire Obtalhed salhe expressly included by reference as useable in the forma- Stufl whlch would he Ohtalned by first coupling into the tion of the dyestuffs of our invention free amlnonaphthol and then condensmg the azo dyestuff The azo dyes represent probably the la rgest class of wrth the trrazme compound. S1m1lar ly, the halogenated trrazlne compound may be reacted wrth one amino group stuffs and the class g1v1ng the greatest flexibility 1n strucin an aromatic diamine and the other amino group can be P h Color There, f be used m the dyestufis of our diazotized and coupled to form the azo derivative. These lhvehhoh ah the Variant-ms of 320 fiyes known F as synthetic methods can be illustrated by the following the mohoazo dyes the the tnsazo the tetraklsazo equations. In the first, chlorotoluidinesulfonic acid is dithe mordaht dyes, the Stllhehe dyes, the PYTaZOlOne and azotized and coupled with H-acid to form the azo dye and thialole y e the like, 80 long as the restrictions are this is then condensed with M-(dichlorotriazinyl)benzoyl met of a primary or a se nd y amino, group through chloride to give the dichlorotriazinylbenzoylamido azo which they can be attached to the triazine ring. dye.

COC1

SOZNa SO Na OH NH:

-NH2 N=N HAcrd or (ham o1 Naots- S0aNa N N CH3 H3 o1- -o1 SO3N8 OH NH-CO Cl- NZl-OJS- SOzNa I ?O:Na 0H I;THLN)-NH OH tl3-O Na N=N N=N Ol- NaO3S -SO3N& NaOaS- -S0sNa -Cl CH CH3 from Z-amino-S-chloro-4-toluenesulfonic acid coupled to Alternatively, the same dyestuff can be prepared by reacting H-acid with M-(dichlorotriazinyl)benzoyl chloride and coupling the reaction product with chloroto- H-acid (8-amino-1-naphthol-3,6-disulfonic acid) is linked luidinesulfonic acid (CTS) diazo.

A third alternative way of preparing the dyestuffs used ing equation in which p-aminoacetanilide is reacted with in our invention in which the dyestufI residue attached the dichlorotriazinylbenzoylchloride, the acetyl group is to the triazine as an azo dye, is illustrated in the follow- 45 hydrolyzed off, and the liberated amino group is diazotized and coupled into Schaeffer acid:

0113c ONH-O-NHZ oo or 01130 ONHQ-NH-O o- NH; N I N CI-kN -01 c1-L -c1 g CHzCONH-ONH-CO- zQ schaeffer diazo Acid N N N N t we? N @3 m HOaS Obviously, if there are further amino groups in the completed dye molecule, or if the dye molecule is capable of further coupling disazo, trisazo and tetrakisazo dyestuffs can be readily prepared, either before or after the diaminotriazinyl radical is placed upon an amino group in the dyestuff residue.

The preparation of the azo dyes may be carried out under conventional conditions, whether the azo dye is prepared first and then reacted with the halogenated carboxyphenyltriazine to form the dyes of our invention, or whether the triazine compound is reacted with either the diazo component or the coupling component and the azo dye is then subsequently synthesized. The reaction of the azo dye or its fragments with the various halogenated carboxyphenyltriazines may be carried out under various conditions. For example, either aqueous or non-aqueous conditions can be used. The reaction under aqueous con ditions is carried out in the presence of an acid-binding agent, such as sodium carbonate or potassium carbonate to take up the hydrogen chloride evolved. In a nonaqueous system, if the azo dye contains sulfonic groups, an amine salt of the azo dye, which will confer solubility in an organic solvent, is conveniently used. Such an amine salt as the di-o-tolylguanidine salt is quite conveniently used in the reaction with the carboxyphenyltriazine derivatives. Where there is no water solubilizing group in the azo dye, a non-aqueous system is preferred.

The azo dye residues of the new triazine dyes which form our invention are derived from various diazo components and coupling components. Examples of the amines which may be used for the diazo components are:

aniline o-nitroaniline rn-nitroaniline p-nitroaniline o, m, and p-chloroaniline 2-nitro-4-chloroani1ine Z-amino-S-nitrotoluene 4-amino-3-nitrotoluene 2-arnino-4-nitrotoluene Z-amino-S-chlorotoluene 2-amino-4-chloroto1uene 2-amino6-ch1oroto1uene 2,5-dichloroaniline 3,4-dichloroaniline 3-amino-4-chlorotoluene o-anisidine 3-nitro-4-methoxyaniline 4-nitro-2-methoxyaniline 2-nitro-4-ethoxyaniline dianisidine 4-arnino-2,S-diethoxybenzanilide 4-amino-2,5-dimethoxybenzophenone lbenzidine (including the monoacetyl derivative) tolidine 4-chloro-2-methoxyaniline 2,4-dimethoxy-S-chloroaniline 4-amino-Z-methoxy-S-chlorobenzanilide l-naphthylamine l-aminoanthraquinone 1-amino-3-chloroanthraquinone 3-amino-4-methoxybenzenesulfonedimethamide 4-methoXy-3-aminophenyl ethyl sulfone 5-benzamido-2,4-xylidine 4-methoXy-4'-aminodiphenylamine 4-aminodiphenylamine 4-chloro-2-aminodiphenyl ether 4,4'-dichloro-2-aminodiphenyl ether o-aminodiphenylamine 5methyl-4-methoxy-2-amino-2-chloro-4'-nitroazobenzene 4'-aminodiphenylaminol-azotoluene 2-amino-4-sulfodiphenyl ether Z-amino-2-methy1-4-sulfodiphenyl ether 4-aminoazobenzene 4-aminoazobenzene-4'-sulfonic acid 4-aminoazobenzene-3,4'-disulfonic acid orthanilic acid S-methyl-orthanilic acid 2-amino-5-chloro-4-toluenesulfonic acid 4-chloroaniline-Z-sulfonic acid aniline-2,5-disu1fonic acid 4-chloro-S-methyl-2-anilinesulfonic acid 2-amino-4-rnethoxybenzenesulfonic acid 2,4-dimethylaniline-6-sulfonic acid 2-amino4-trifiuoromethylbenzenesulfonic acid 3,4-dichloroaniline-6-sulfonic acid 3,5-dichloroaniline-6-sulfonic acid 3-methoxyaniline-6-sulfonic acid 4-methylani1ine-6-sulfonic acid dehydrothiotoluidinesulfonic acid 2-aminonaphthalene-4,8-disulfonic acid Z-aminonaphthalene-6-sulfonic acid 2-aminonaphthalene-6,8-disulfonic acid l-aminonaphthalene-4,5,6 and 8-sulfonic acid Z-aminonaphthalene-5,7-disulfonic acid 2-arninonaphthalene-7-sulfonic acid p-phenylenediamine 3,3'-dichlorobenzidine 3 ,3 -benzidinedisulfonic acid 2,2'-dichloro-3,3'-dimethoxy-4,4-diaminodiphenyl 3-aminopyridine S-aminoquinoline 4,4-diaminostilbene-2,2'-disulfonic acid 3,8-diaminodibenzothiophene and its sulfonic acid Examples of the compounds which may be used as the coupling components are:

Aniline o-toluidine m-toluidine 1 1 2,5-dimethylaniline o-anisidine m-anisidine Z-methoxy-S-methylaniline 2,5-dimethoxyaniline N-methylaniline N-methyl-o-toluidine N-methyl-m-toluidine N-ethyl-o-toluidine N-methyl-Z-methoxy-S-methylaniline N-ethyl-Z-methoxy-S-methylaniline N-methyl-m-anisidine N-ethyl-m-anisidine l-amino-8-naphthol-6-sulfonic acid 1-amin0-8-naphthol-3,6-disulfonic acid 1-amino-8-naphthol-4,6-disulfonic acid 1-methylamino-8-naphthol-6-sulfonic acid 2-arnino-5-naphthol-7-sulfonic acid Z-methylamino-S-naphthol-7-sulfonic acid 1-amino-8-naphthol-2,4-disulfonic acid 1-amino-8-naphthol-4-sulfonic acid .3-methyl- -pyrazo1one 1-phenyl-3-methyl-5-pyrazolone 1-(4-sulfophenyl) -3 -methoyl-5-pyrab olone 1- (4-chlorophenyl -3 -methyl-5 -pyrazolone 1-phenyl-3-carbethoxy-5-pyraz01one acetoacetanilide 4-sulfoacetoacetanilide bis-acetoacetbenzidide bis-acetoacettolidide acetoacettolidide beta-hydroxynaphthoic acid arylides of various hydroxy naphthoic acids such as 3-hydroXy-2-naphthanilide 3-hydroxy2-naphthoyltoluidide and the like.

Many other coupling components and diazo components are described in the various chapters of Venkataraman covering the azo dyes, found on pages 409-704 of that treatise. Any combination of these components which produces an azo dye having an amino group capable of reacting with the halogenated carboxyphenyltriazine derivative (i.e., a primary or secondary amino group) is capable of forming the dyesuifs of our invention Which contain azo dye residues. A great many such dyes are specifically disclosed in these chapters. As stated above, the amino group may be either a primary or an secondary, but not a tertiary amino group, there must be one hydrogen capable of replacement by the carboxyphenyltriazine radical.

(B) Vat dye residues The various anthraquinone and other polyquinonoid structures which are known collectively under the generic term of vat dyes, are described in Venkataraman in Chapters 27-34, inclusive, pages 803-1058. To the extent that anthraquinones and other vat dye structures are available having a primary or a secondary amino substituents, they are readily useable in the dyestufls of our invention in the same Way as the azo dyestufi' residues.

Examples of some of the anthraquinonoid compounds which may be used to form the dyestulf of our invention are:

l-aminoanthraquinone Z-aminoanthraquinone 2-methyl-l-aminoanthraquinone 2-amino-3-chloroanthraquinone 4-methyl-1-aminoanthraquinone 6-methyl-l-aminoanthraquinone 3-ch1oro-l-aminoanthraquinone 5-chloro-l-aminoanthraquinone S-benzamido-l-aminoanthraquinone 4- and 5 -aminoanthraquinone-1 (N) 2-benzacridones 4- and S-aminoanthraquinone-l(S)2-thioxanthrones 4-aminoanthrapyrimidine 4-amino-2,3-benzanthraquinone 1,9-pyrazolanthrone aminodibenzanthrone 4-aminoanthraquinone-1 (N) ,2,1' (N) 2'-carbazo1e 1,4-diamino-2-(2,3-anthraquin0nethiazolyl) anthraquinone 1,9-thiazoloanthrone 1-chloro-2-aminoanthraquinone 2-amino-3-methylsulfony1anthraquinone 2-amino-6-benzamidoanthraquinone 1-amino-4- (4'-aminopheny1amino -anthraquinone- 2,3'-disulfonic acid 1-methylamino-4- (4'-aminophenylamino) -anthraquinone-2,3'-disulfonic acid 1-amino-4- 4-aminophenylamino) -anthraquinonedisulfonic acid 1-amino-4- (4'-aminophenylamino) -anthraquinone- 2,3 ,5-trisulfonic acid 1-amino-4-(4' [4"-aminopheny1azo]anilino)- anthraquinone-2,5,2"-trisulfonic acid l-amino-4- (4 [4"-arninopheny1] anilino) -anthraquinone-2,5,3"-trisulfonic acid 1-amino-4-(4-aminophenylamino)-anthraquinone- 3-sulfonic acid 1-amino-4- (3 '-aminophenyla-mino) -anthraquinone- 4'-sulfonic acid 1-amino-4- (4'-aminophenylamino -anthraquinone- 2-su1fonic acid 1-amino-4- (3 -amino-4-methylphenylamino) anthraquinone-Z-sulfonic acid 1-amino-4-(4-amino-3'-methylphenylamino)- anthraquinone-2-sulfonic acid 1-amino-4-(3'-amino-4,6'-dimethylphenylamino)- anthraquinone-Z-sulfonic acid 1-amino-4- (4'-aminophenylamino) -anthraquinone- 3-sulfonic acid diethylamide In addition to this list there is a class of anthraquinonoid compounds which may be represented by the formula:

in which M is hydrogen or sulfonic acid and A represents an arylene radical which may be further substituted with acidic groups such as sulfonic acid or carboxylic acid and where R is hydrogen, alkyl, aralkyl or cycloalkyl. The aromatic diamine proportion of this molecule NHANHR-- may be derived from various aromatic diamines such as:

m-phenylene diamine p-phenylene diamine benzidine dichlorobenzidines 4,4'-diaminoazobenzene m-phenylenediamine-4-sulfonic acid benzidine-3-sulfonic acid p-phenylenediamine-Z-sulfonic acid 4,4-diaminoazobenzen-Z-sulfonic acid p-phenylenediamine-Z-carboxylic acid and the like.

Of especial interest along this line are the acid anthraquinone dyes described in Chapter 29 of Venkataraman, pages 834-860, wherein a large number of compounds having solubilizing groups are described.

Vat dye residues without solubilizing groups may be selected from any of the amino-substituted vat dyes or vat dye intermediates shown in pages 803-1058 of Venkataraman. When vat dyes are desired, at least two 13 vat dye' residues must be linked to the carboxyphenyltriazine nucleus.

(C) Phthal-ocyanine residues The phthalocyanine structure is known to be a highly In general, the carbonyl chloride group on the phenyl portion of the molecule will react with an amine first. When only one mole of an amino dyestufl? is used this is the chlorine which is replaced and the resulting product is a dichlorotriazinylbenzamide. With the use of larger Stable and highly eelofed chemical Stfllethfeuse quantities of dyestuff amine' and of more drastic temperaiIl Pigments is Well known and is described 111 e tures as described above, the triazine chlorines are readily katammah Chapter Pages 1118-1142- Vafiolls amlho replaced. Thus, if a second different amine is used a mixed substituted phthalocyanines are known including y dye is obtained. This can be done ste wise, so that d ewhich are sulfonated or carboxylated or otherwise subt fl h i t or th i o d t ff residues Stitllted y an acid groupihg- Such Compounds can be prepared, the amino dyestuff residues being the without solubilizing groups are readily usable in preparing Same or diiferent the dyes of Our in en ion. e amino gr p y h In the preparation of the dyestuffs of our invention, as directly 011 the phthaleeyahihe rings y y he h an alternative, the carboxyl chloride substituents can be a Side-Chain Such as an amhlomethyl P- The letter 15 15 reacted with amines other than dyestuff amines, provided Preferred heeallse of the ease of P p Sihee Such the chlorines on the triazine ring are replaced by at least PfethletS can he P p from the phthaloeyanihe itself one amino dyestuff moiety. Such other amines include by treatment with methylolphthalimide and sulfuric acid di lk l i h as di th l i di h l i dias described in the United States Letters Patent 2,761,868 propylamine and the like, piperidine and morpholine, to y- Sulfonation can Occur at the Same time under However, when the triazine chlorines or bromines are the P p Conditions and D to foul amihomethyl g p then replaced, they must be replaced'by amino dyestutf can readily be introduced as Wel1 as p to four Sulfohie residues. If the triazinc chlorines remain on the molecule, acid groups. Also phthalocyanine carboxylic acids can be i order t h a dyest fi th b l hl id b. amihomethylated in the same manneri i rly, the stituent must have been reacted with an amino dyestuif. nuclear substituted phthalocyanines such as those con- A of h intermediates d ib d i preceding taining one to four chlorines can be sulfonated and/o1 tio f thi e ifi ation an be u d to giv dye t if by aminomethylated. The total number of substituents should replacing h h l present, Any h d i h i n eXCeed nine in phthalocyanine molecule The ing can be converted into halogen and used for further re- Phthalocyahihe in the form of pp Cobalt, Illekel placement by amino dyestuif if such is desired. That is, or other metal complexes in Which form y e also the use successively of several different dyestulfs permits Used in Our ihventioh- When phthaloeyahhleS Wlthoht the obtaining of a wide variety of shades. One may have SOhlhihZihg groups are used, the Products are P g mixtures of different amino vat dyes, different azo dyes, or y, unless a SeeOnd dye of another class is also comdifferent aminophthalocyanines. One can also have mixbined with the triazine derivatives. tures of amino vat dyes, amino azo dyes or of three dif- (D) other dyesmfi classes ferent kinds of dyestuffs. In general, when one has at least two azo groupings, one applies the compounds like The other classes of dyestuffs Whlch are known are an azo dyestutf. Similarly, if one has at least two amino geherahy of less hhportahce than the three clases vat dye structures linked to the phenyltriazine nucleus, scribed above. However, they may have the necessary one uses the product as a vat dye. If the amino dyestuif eomhlhatloh 9 ah held ghOhPlhg and a Phmary or a substituents in the dyestuffs of our invention have at least secohhary ammo h i and when they do e be two solubilizing groups, the product can be applied as an used In the pregaratlon dyestuffs of P mventlonacid dye. If they have no solubilizing groups, the product Compounds having the necessary prerequ sites can be may used as a pigment unless it can be applied as a found amhhg the Xahthehe acndlhe and azlhe dyestuffs, vat dye. The dyestuifs which have chlorines remaining in deseflhed h Pages 740-795 of Vehkataramhh the molecule may also be applied by techniques involving A eohlplete hhe of the dyes of our lhvehhoh W111 the reaction of these chlorines with fibers. The various necessarily include azo structures, vat structures and types of dyestuffs which form our invention and their phthalocyahlhesa at least, 111 Order t get the mlmmum modes of application can be illustrated by the following Vanety heeded Colors and Properhestable in which X, Y and Z refer to the general formula (III) PREPARATION OF DYESTUFFS The dyestuffs of our invention are prepared by the COX ordinary acylation procedures by which carboxylic chlorides are reacted with amines and triazinyl chlorides are reacted with amines. These procedures will vary general- I 1y, depending on the amines used and consequently, the

. N N procedure modifications used Will depend upon what I I amino dyestufi residue is being introduced into the molez cule. N

X Y Z Used in the usual manner for Aminoazo dye (sulfonated) Aminoazo dye (sulfonated). Arninoazo dye (sulionated) Acid dye.

Do. Aminoazo dye Aminoazo dye Pigment (possibly acid dye it sufficiently soluble). Aminoazo dye ..do ..do Pigment. Amino vat dye. Amino vat dye... Amino vat dye Vat dye or pigment.

Do ..do Aminoazo dye Do. Amino vat dye (sullonated) Amino vat dye (sulionated) Aminoazo dye (sulf0nated).- Acid dye or vat dye. Aminophthalocyanine. Amino vat dye Amino vat dye Vat dye or pigment.

D0 Aminophthalocyanine Aminoazo dye Pigment. Aminophthalocyanine Aminophthalocyanine Aminophthalocyanine Acid dye.

(sulfonated) (sulfonate d) (sulfonated) Am no-coupling component Amino coupling component... Amino coupling component... Azoic dye with diazo developer. Am no-dlazo component Am no diazo component Amino diazo component Diazo developer with naphthol. Amine Amino vat dye Amino vat dye Vat dye. Aminoazo dye (sullonated). Aminoazo dye (sulfonated) Chlorine dye or dye reacting with Do Chlorine d0.. 1% Chlorine Amino vat dye ..do- Dye reacting with fiber.

Do- Ammoazo dye (sulfonatedL..- Aminoazo dye (sullonated)...

Acid dye or dye reacting with fiber.

Other variations in the possible combinations will be obvious to the dye chemist.

Our invention can be illustrated by the following examples in which parts are by weight unless otherwise specified and parts by volume are to parts by Weight as milliliters are to grams.

EXAMPLE 1 A mixture of 67.5 parts of dicyandiamide, 560 parts of acetone and 5 parts of water is cooled to C. 64 parts of potassium hydroxide is added and, while stirring at 0 to C., there is added dropwise, gradually a solution of meta-toluyl chloride prepared by chlorination of 49.7 parts of m-toluic acid in 80 parts of acetone. After stirring for 2 hours, the temperautre is allowed to rise gradually to C. The mixture is then drowned in 2500 parts of water, containing 50 parts sulfuric acid. The solid precipitate is removed by filtration and washed acid-free.

The corresponding p-toluyl derivative is obtained by starting with p-toluic acid. The corresponding Z-methoxy- S-methyl-benzoyl derivative is obtained by starting with 2-methoxy-5-methyl-benzoyl chloride.

EXAMPLE 2 The meta-toluyl dicyandiamide prepared as described in Example 1 is added to 500 parts of water and 120 parts of 5 N hydrochloric acid. The mixture is heated at the reflux temperature for four hours and, after cooling, the solid product is removed by filtration, washed and dried, giving the m-toluyl biuret.

p-Toluylbiuret is obtained in similar fashion by hydrolysis of p-toluyldicyandiamide, as is also 2-methoxy-5- methylbenzoylbiuret.

EXAMPLE 3 To a solution of 60 parts of potassium hydroxide in 1100 parts of water is added 42.7 parts of m-toluylbiuret prepared as described in Example 2. After stirring and heating to 50 C., the mixture is allowed to stand overnight. It is then heated to 50 C. with 5 parts of decolor- 16 izing charcoal. After filtration, the filtrate is acidified with concentrated hydrochloric acid, cooled and stirred. The product is removed by filtration, washed and dried, giving the m-toluguanamide, melting point 274-276 C.

The p-toluyl guanamide is obtained in similar manner starting with p-toluylbiuret, and similarly 2-methoxy-5- methylbenzoguanamide is obtained from 2-methoxy 5- methylbenzoyl biuret.

EXAMPLE 4 Q-ooou To a solution of 21.8 parts of potassium hydroxide and 1500 parts of water at 50 C. is added 35.7 parts of m-toluguanamide (2 m-tolyl-4,6-dihydroxy-s-triazine). After stirring and increasing the temperature to 60 C., complete solution is obtained. To the solution is then added 55.5 parts of potassium permanganate in small proportions over a period of many hours, a fresh portion of permanganate being added only when a test spot on paper shows no permanganate color. The slurry is then filtered to remove manganese dioxide. The filter cake is washed with hot water and any color in the filtrate is discharged by the addition of a small amount of sodium bisulfite. The clear colorless filtrate is then acidified at 30 to 40 C. with about 60 parts of concentrated hydrochloric acid and the white crystalline precipitate is removed by filtration, washed with water and dried.

The following products are prepared using a procedure similar to that described above but using an appropriately substituted methyl-benzoguanamide:

o-Carboxybenzoguanamide m-Carboxybenzoguanamide p-Carboxybenzoguanamide Z-methoxy-5-carboxybenzoguanamide EXAMPLE 5 O 0 Cl N N CILNJCI To 55 parts of chlorobenzene is added 9.4 parts of meta-carboxybenzoguanamide. With stirring is then added 25 parts of phosphorous pentachloride and 0.2 part of triethylamine sulfur trioxide complex. The mixture is heated with stirring at the reflux temperature until the reaction is substantially complete. After several hours at the reflux temperature, about 0.5 part of phosphorus oxychloride triethylamine complex is added. A small amount of solid material is removed by filtration. The chlorobenzene is removed from the filtrate by vacuum distillation, giving the crude product which is purified by recrystallization from methyl cyclohexane.

17 The following acid chlorides of 2-carboxyphenyl-4,6- dichlorotriazines are prepared using a similar procedure:

o-Car-boxy p-Carboxy Z-methoxy-S-carboxy By using equivalent amounts of phosphorous pentabromide and phosphorus oxybromide, the corresponding bromo derivatives are obtained.

EXAMPLE 6 og N N 6 NHXIN/!NH To 82 parts of nitrobenzene is added 2.9 parts of the acid chloride of 2 (m carboxyphenyl) 4,6 dichloros-triazine and 6.7 parts of l-aminoanthraquinone. The mixture is heated with stirring. A reaction starts at about 60 C. with evolution of hydrochloric acid. The heating is continued and at about 130 C., a second reaction starts and the slurry thickens. An additional 55 parts of nitrobenzene is added. The heating with stirring is continued at 140 C. to 150 C. until the reaction is substantially complete. The mixture is cooled. Two parts of sodium carbonate is added and the mixture is warmed to 60 C. The solid product is then removed by filtration, washed and dried. The product dyes cotton a yellow shade from a claret vat.

EXAMPLE 7 The procedure of Example 6 is followed, using an equivalent quantity of 1 amino 3 chloro-anthraquinone in place of the l-aminoanthraquinone, to give a dye which dyes cotton a bright yellow shade from a brown vat.

EXAMPLE 8 The procedure of Example 6 is followed, using an equivalent quantity of 1 amino 4 benzamido anthraquinone in place of the l-aminoanthraquinone, to give the above product which dyes cotton a red of excellent fastness.

EXAMPLE 9 O NH-L NH O The procedure of Example 6 is followed, using the acid chloride of the para-carboxy compound in place of the m-carboxy compound, and using 1 amino 4 chloroanthraquinone in place of the l-aminoanthraquinone, to give the above product which dyes cotton a reddish shade of yellow.

EXAMPLE 11 The procedure of Example 6 is followed, using the acid chloride of the p-carboxy compound in place of the m-carboxy compound, and using 1-amino-4-benzamidoanthraquinone in place of l-aminoanthraquinone. The product dyes cotton a red color.

EXAMPLE 12 -C O-A (where A is an a-aminoanthroquinone residue linked through the amino nitrogen.)

The procedure of Example 6 is followed, using the acid chlori e of 2-(2-111eth0Xy=5=carb0Xyphenyl) 4,6=dichlor- 20 s-triazine in place of the acid chloride of 2- (m-carboxyphenyl)-4,6-dich1oro-s-triazine, and using the various aminoanthraquinones shown below.

Amine: Dye Color l-arninoanthraquinone Yellow. 1-amino-4-benzamidoanthraquinone Red. 1-amino-4- 3-methylsulfonylbenzamido anthraquinone Red. 1-amino-4-(m-methoxybenzamido)-anthraquinone Red.

EXAMPLE 13 /C2H5 C0N CzHs T T NQNANH 0 II II To 2.9 parts of the acid chloride of Z-(m-carboxyphenyl)-4,6-dichloro-s-triazine in 70 parts of nitrobenzene is added gradually 0.75 part of diethylamine in 10 parts nitrobenzene. Then one part of triethylamine is added and the mixture is stirred and warmed gradually to 50 C. To the mixture at this temperature is then added 4.4 parts of l-aminoanthraquinone. The whole is then heated gradually with stirring to a temperature of 135 C. and is then held at this temperature until the reaction is substantially complete. Two parts of triethylamine is then added and the solid is removed by filtration. The product dyes cotton yellow.

Similar products are obtained when equivalent amounts of dipropylamine, dioctylamine, morpholine, or piperidine are substituted for the diethylamine.

EXAMPLE 14 A mixture of 3.8 parts of 2-amino-7-chloro-3,4- phthaloylacridone in 110 parts of nitrobenzene is stirred at 185-190 C. until solution is achieved. It is then cooled to 40 C. and 219 parts of the acid chloride of Z-(m-carboxyphenyl) 4,6 dichloro-s-triazine is added. The mixture is heated gradually to C. and is then stirred at IOU- C. until the reaction is substantially complete.

21 Then 4.5 parts of l-aminoanthraquinone and 40 parts nitrobenzene are added and the whole is heated at 145- 150 C. with stirring until the further reaction is substantially complete. The solid product is removed by filtration at 60 C., washed and dried. The product dyes cotton a blue-grey color.

g 6011: (EH 2) To 4.7 parts of 5,8-dibenzamido-l-aminoanthraquinone slurried in 110 parts of nitrobenzene is added 2.9 parts of the acid chloride of Z-(m-carboxyphenyl)-4,6-dichloro-s-triazine. The mixture is very gradually heated to 120 C. Then 5.1 parts of l-amino-4-methoxyanthraquinone and 2 parts of dimethyl cyanamide are added and the mixture is stirred at 125130 C. until the reaction is substantially complete. The solid is removed by filtration, washed and dried. It dyes cotton a red color.

EXAMPLE 16 O -O IIIH NH C O 0 [j and I T KT CIL Cl L N/ l e? (i I'm I IH ti C5H5-CO C0 C5115 To a slurry of 2.25 parts of l-aminoanthraquinone and 110 parts of nitrobenzene at 30 C. is added 2.9 parts of the acid chloride of 2-(p-carboxyphenyl)-4,5-dichloro-striazine. The mixture is heated to 47-48 C. gradually and it is then stirred at 48-55 C. until the reaction is substantially complete. The solid dichlorotriazine compound is removed by filtration, washed and dried.

A mixture of 3.3 parts of the yellow dichlorotriazine compound and 4.8 parts of 1-amino-4-benzamidoanthraquinone in 110 parts of nitrobenzene is heated gradually 22 to C. with stirring. The mixture is stirred at 140 C. to C. until the reaction is substantially complete. The solid product is removed by filtration, washed and dried, giving 6.6 parts of product which dyes cotton a brick red shade from a red-violet vat.

EXAMPLE 17 and A slurry of 3.8 parts of 2-antino-7-chloro-3,4-phthaloyl acridone in 110 parts of nitrobenzene is heated at 195- 200 C. until the acridone has dissolved. It is then cooled to 40 C. and 2 parts of the acid chloride of 2-(p-carboxyphenyl)-4,6-dichloro-s-triazine dye can be isolated by cooling, filtering and washing. It dyes cotton a blue-gray shade from a violet vat.

To the mixture containing the dichlorotriazine dye is added 5.1 parts of 1-arnino-3-chloro-anthraquinone and 2.2 parts of chlorobenzene. The mixture is heated at -175 C. until the reaction is substantially complete. It is then cooled. At 40 C. the solid product is removed by filtration, washed and dried. The product dyes cotton a green color from a violet brown vat.

EXAMPLE 18 The procedure of Example 17 is followed using an equivalent amount of l-aminoanthraquinone in place of the 1-amino-3-chloroanthraquinone. The heating in the second step need only be to 150 C. The product dyes cotton an olive green shade.

. 23 EXAMPLE 19 To 100 parts of molten phenol is added 5.1 parts of 2- (1,4 diamino-Z-anthraquinonyl) -anthra- (2,3-d) -thiazole- 5,10-dione. The mixture is heated to the boiling point to remove water and is then cooled to 75 C., at which temperature 2.9 parts of the acid chloride of 2-(4-carboxyphenyl)-4,6-dichloro-s-triazine is added. The mixture is slowly warmed to 100-105 C. and is then stirred at this temperature until the reaction is substantially complete. To it is then added 4.5 parts of l-aminoanthraquinone and the mixture is then stirred at 135-150 C. until the second reaction is substantially complete. The solid is removed by filtration and slurried in dilute sodium carbonate solution at about 80 C. The solid is removed by filtration, Washed and dried. The product dyes cotton green shades from a brown-violet vat.

A mixture of 3.2 parts of the acid chloride of 2-(2-methoxy-S-carboxyphenyl) 4,6 dichlorotriazine and 1.75 parts of morpholine in 65 parts of o-dichlorobenzene is warmed to 65-75 C. until the reaction is substantially complete. A small residue is removed by filtration and to the filtrate is added 6.8 parts of 1-amino-4-benzamidoanthraquinone and an additional 55 parts of o-dichlorobenzene. The mixture is heated with stirring at l30-135 C. until the reaction is substantially complete. The solid product is removed by filtration, washed and dried. The product dyes cotton a red color.

24 EXAMPLE 21 OHaOHzOH CON OHzCHzOH OH O- i T NH N u N n A slurry of 3.2 parts of the acid chloride of 2-(2- methoxy-S carboxyphenyl) 4,6 dichlortriazine and 2.1 parts of diethanolamine in parts of acetone is heated at 50-55 C. until the reaction is substantially complete. A slight residue is removed by filtration and 4.5 parts of l-aminoanthraquinone and parts of o-dichlorobenzene are added. Acetone is removed by distillation to a temperature of about 138 C. and the mixtures then stirred at 130-140 C. until the reaction is substantially complete.

The solid material is removed by filtration, Washed Well and dried. The product dyes cotton a reddish yellow shade.

EXAMPLE 22 S OsNa A solution of 5.4 parts of disodium salt of 1-amino-4- (4-aminoanilino)-anthraquinone 2,2 disulfonic acid in 125 parts of water at 10 C. is added gradually with good agitation to a solution of 2.9 parts of 2-(m--chlorocarbonylphenyl)-4,6-dichloro-s-triazine in 35 parts of acetone at 10 C. 8.4 parts of a 10% NaHCO solution is then added to the mixture and the mass stirred at 5l0 C. until the reaction is substantially complete, While adding two parts more 10% NaHCO to maintain faint alkalinity. To the dark blue slurry is then added 25 parts sodium chloride and after an hour, the solid is filtered at room temperature and the cake washed with a solution of 25 parts NaCl, 15 parts NaH PO -H O and 6 parts Na HPO in 125 parts Water. The wet cake is then dried at 20-45 C. The product dissolves in water with a greenish-blue color and in concentrated H SO with a blue color. It dyes cotton a blue shade of excellent wash fastness when applied by the procedure of Example 24.

I EXAMPLE 23 01 N I I O1 (IO-NH 011 (RH;

N=N C1 NaO S- S0 Na SO Na A 6.4 part portion of the trisodium salt of the aminoazo dye produced by diazotizing 4-chloro-5-methyl-aniline-2- sulfonic acid and coupling the diazo compound with an alkaline solution of H Acid, is dissolved in parts of water and the mixture is cooled to 5 C. The resulting solution is poured gradually with stirring into a solution of 2.9 parts of 2-(m-chlorocarbonylphenyl)-4,6-dichloros-triazine dissolved in 35 parts acetone and cooled to 5 C. parts of a 10% NaHCO solution is added and the mixture stirred while it is gradually warming to 10 C. Then 10 parts more 10%. NaHCO is added and the stirring is continued several hours at C. The mixture is then warmed to C. and 25 parts sodium sulfate is added. The mixture is stirring at room temperature to get homogeneity. The slurry is then filtered and the filter cake is washed with 20 Na SO solution. The Wet cake is dried at 20 to 45 C. the product dissolves in concentrated sulfuric acid with a bluish red color and in water with a red color. It dyes cotton bright bluish-red shades when applied by procedure of Example 24.

EXAMPLE 24 A dye solution is prepared by dissolving 2 grams of the dye of Example 23 in 100 grams of water containing 0.3 gram of surface active agent (polyoxyethylene esters of mixed fatty and resin acids). A piece of cotton fabric is padded in this solution at about 1 60175 F. and is then removed and passed through rollers adjusted to allow an 80% pick up. The cloth is then dried.

The piece of dried fabric is then padded in 100 ml. of a chemical pad bath containing grams of sodium chlo ride and 5 ml. of 30 B. sodium hydroxide solution. It is removed and passed through rollers adjusted to allow about a 50% pick up. The temperature of this pad bath should be at about room temperature, about 20 C. The fabric is then steamed for a short time at 335 F.

Non-bonded dye is then removed from the fabric by soaping at the boil. This involves heating at the boiling point in a solution containing about 2 grams per liter of an oleate soap. The cotton fabric is dyed a bluish-red color of excellent wash fastness.

EXAMPLE 25 The procedure of the second paragraph of Example 16 is followed using /2 an equivalent of monoaminomethylphthalocyanine in place of 4-benzoylamino-l-aminoanthraquinone. The product is a green dye when dyed by the procedure of Example 24.

EXAMPLE 26 The procedure of Example 16 is followed using an equivalent amount of monoaminophthalocyanine for the 26 benzoylamino l-aminoanthraquinone. The product is a green blue pigment.

EXAMPLE 27 N N CPL J-Cl Pcy=pl1thal0cyanine The procedure of the first paragraph of Example 16 is followed using triaminomethylphthalocyanine in A the equivalent amount of the useage of aminoanthraquinone. The product is a dyed cotton blue by the procedure of One equivalent weight of the product of Example 5 is dissolved in approximately 6 times its weight of mono- EXAMPLE 28 chlorobenzene. To this mixture is added one equivalent weight of water and the mixture is stirred at 60-70 C. until hydrolysis of the carboxy chlorine is complete. Slightly over two equivalent weights of l-aminoanthraquinone is then added and the mixture is heated gradually to 140 C. It is stirred at 140-150" C. until the reaction is complete. The mixture is then cooled and an excess of a one equivalent of thionyl chlorine is then added. The mixture is then heated at -120 C. until the reaction is substantially complete. The product separates from the reaction mixture when it is cold. It is isolated by filtration and washing.

EXAMPLE 29 One equivalent weight of the product of Example 5 is added to approximately 6 times its weight of monochloro benzene. Approximately two equivalent Weights of water is then added and the mixture is heated slowly to approximately C. until hydrolysis of two of the chlorines is substantially complete. The chlorobenzene is then removed by vacuum distillation. The product is then used in the procedure of the second paragraph of Example 16 using this product in equivalent quantity in place of the dichloro product used there and half the quantity of 1- amino-4-benzamido anthraquinone. The product of this reaction is then used in the procedure of Example 5 using only /3 the equivalent quantity of phosphorus pentachloride. The dichloro compound is recovered by filtration from the chlorobenzene solution and is washed with alcohol and then dried.

27 28 EXAMPLE 30 (m-carboxyphenyl) 4 (1 anthraquinony1amino)-6- chloro-s-triazine, which on retreatment by the process of COOH Example 5 gives the corresponding 2-(m-chlorocarbonylphenyl) triazine compound.

5 EXAMPLE 31 The procedures of the preceding examples are followed N N using the proper equivalent quantities of the appropriate I carboxyphenyl triazine intermediate and the appropriate 10 amino dyestufi to give the dyestufis shown in the following table in which Ar, X, Y and Z refer to the general A one-mol quantity of the product of Example 5 is formula heated to 50-60 C. in 50 parts of chlorobenzene to which .Ar-COX a one-mol quantity of water and a three mole quantity of l pyridine has been added. On cooling, the carboxyphenyl dichlorotriazine separates. 0 I

This product, when used in the procedure of Example 6 z-L Y with half the quantity of aminoanthra-quinone, gives 2- N Ar=CO X Y Z O O 1TIH CIJI-I Same as X Same as X.

| NZLOQS S OaNa Same as above Same as above Same as X C1.

D0 do CI 01 D0 do Br Br.

0 CO 1 01 01130 q N=N O-Ou-O I NaOaS- N=N S OaNa IIT-CHa Same as above Same as above (I? IFH- Same as Y.

G Br- ('11 1%111 3H 1 C1 C0 N=N- N=N S O3Na C] Cl.

Ar=CO X Y Z O O -NHc0pper phthalocyanine sulfonic acid I IIH (H1 (3111 Same as Y.

-N=NC C1 NaO S -s OaNa SOaNa Same as above 01.. Same as above 01.

Same as above O1 01.

l I 9 1| 0 NH Same as above. ?O Na Cl 01-.

1 N=N -0 O-NHC -NH I S OsNa We claim: References Cited 1- Th$ dye of the formula ,D 2,729,638 1/1956 Joyce 260249 40 3,060,180 10/1962 Staeuble et a1. 260249.5 3,133,059 5/1962 Frederick 260153 X A HENRY R. JILES, Primary Examiner 1 F 4r R. T. BOND, Assistant Examiner d Olin/T01 3 US. 01. X.R.

in which Pcy is phthalocyam'ne, said dye being the prod- 8-42, 34, 39; 260-242, 314.5, 146, 153, 249.5, 249.4, uct obtained by condensing three mols of the acid chlo- 249, 247.7 ride of 2-(carboxyphenyl)-4,6-dichloro-s-triazine with 50 one mol of triaminomethylphthalocyanine. 

